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rs794727153

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs794727153(-;-)
Make rs794727153(-;A)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position74182376
GeneSTRA6
is asnp
is mentioned by
dbSNPrs794727153
ClinGenrs794727153
ebirs794727153
HLIrs794727153
Exacrs794727153
Varsomers794727153
Maprs794727153
PheGenIrs794727153
hapmaprs794727153
1000 genomesrs794727153
hgdprs794727153
ensemblrs794727153
gopubmedrs794727153
geneviewrs794727153
scholarrs794727153
googlers794727153
pharmgkbrs794727153
gwascentralrs794727153
openSNPrs794727153
23andMers794727153
23andMe allrs794727153
SNP Nexus

SNPshotrs794727153
SNPdbers794727153
MSV3drs794727153
GWAS Ctlgrs794727153
Max Magnitude0
ClinVar
Risk rs794727153(-;-)
Alt rs794727153(-;-)
Reference Rs794727153(A;A)
Significance Pathogenic
Disease Microphthalmia syndromic 9 not provided
Variation info
Gene STRA6
CLNDBN Microphthalmia syndromic 9 not provided
Reversed 1
HGVS NC_000015.9:g.74474717delT
CLNSRC
CLNACC RCV000174950.1, RCV000413306.1,